| Weight | 155.966 g/mol |
|---|---|
| Formula | C2H5I |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Iodoethane (75-03-6)
Score:
#49 in Physical chemistry
,
#1476 in Physics
,
#4348 in Chemistry
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- Sigma-Aldrich - Iodoethane23.40 - 159.00 USD
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- Catalytic reduction of Iodoethane and 2-Iodopropane at Carbon Electrodes Coated with Anodically Polymerized Films of Nickel(II) Salen (Analytical Chemistry, 1994)
- Reactions of iodoethane, iodopropane, 2-iodopropane, chloroiodomethane adsorbed on silver(111) (The Journal of Physical Chemistry, 1991)
- Catalytic reduction of iodoethane by cobalt(I) salen electrogenerated at vitreous carbon cathodes (Journal of Electroanalytical Chemistry, 1998)
- Palladium-catalyzed trifluoroethylation of terminal alkynes with 1,1,1-trifluoro-2-iodoethane. (Organic Letters, 2013)
- A simple preparation of iodoarenes, iodoalkenes and iodoalkynes by reaction of organolithiums with 2,2,2-trifluoro-1-iodoethane (Tetrahedron Letters, 1999)
- Experimental and predicted volumetric and refractive index properties of ternary mixtures of iodoethane with toluene and alcohols at temperature 298.15 K and pressure 101 kPa (The Journal of Chemical Thermodynamics, 2006)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCCI
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InChIKeyHVTICUPFWKNHNG-UHFFFAOYSA-N
- Pubchem - Iodoethane
- Wikipedia - iodoethane
Ethyl iodide (also iodoethane) is a colorless, flammable chemical compound. It has the chemical formula C2H5I and is prepared by heating ethanol with iodine and phosphorus. On contact with air, especially on the effect of light, it decomposes and turns yellow or reddish from dissolved iodine.
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Iodoethane
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